METFORMIN HYDROCHLORIDE
- Product NDC
- 67296-1711
- 11-digit product format
- 672961711
- Labeler code
- 67296
- Product ID
- 67296-1711_b8dfb680-8a9b-5315-e053-2995a90aa59d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA203769
- Marketing category
- ANDA
- Marketing start
- 2018-01-15
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Biguanide [EPC],Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67296-1711-6 | METFORMIN HYDROCHLORIDE | 60 in 1 BOTTLE | TABLET | 60 | | 10 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1711 | METFORMIN HYDROCHLORIDE TABLET [REDPHARM DRUG, INC.] | 10 | Legacy NDC, 1 package rows | 20240805_96db004b-1752-5f29-e053-2995a90af80e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67296-1711-6 | 67296171106 | 60 TABLET in 1 BOTTLE (67296-1711-6) | 60 tablet | 2019-11-01 | 0000-00-00 | No | No | Current |